1246812-30-5

(Rac)-8-Hydroxy-efavirenz-d<sub>4</sub> Chemical Structure
1246812-30-5

Chemical Structure

(Rac)-8-Hydroxy-efavirenz-d4

  • CAS No.: 1246812-30-5
  • Formula:C14H5D4ClF3NO3
  • Molecular Weight:335.70

IUPAC Name: 6-chloro-4-((cyclopropyl-2,2,3,3-d4)ethynyl)-8-hydroxy-4-(trifluoromethyl)-1,4-dihydro-2H-benzo[d][1,3]oxazin-2-one

InChIKey: OOVOMPCQLMFEDT-LNLMKGTHSA-N

SMILES: C(#CC1C(C1([2H])[2H])([2H])[2H])C2(C(F)(F)F)C=3C(NC(=O)O2)=C(O)C=C(Cl)C3

Biological Activity: rac 8-Hydroxy Efavirenz-d4 is the deuterium labeled rac 8-Hydroxy Efavirenz[1]. rac 8-Hydroxy Efavirenz-d4 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.

Cat. No. Product Name Purity Description Pricing
HY-131422S
(Rac)-8-Hydroxy-efavirenz-d4 rac 8-Hydroxy Efavirenz-d4 is the deuterium labeled rac 8-Hydroxy Efavirenz. rac 8-Hydroxy Efavirenz-d4 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
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HY-131422
(Rac)-8-Hydroxy-efavirenz (Rac)-8-Hydroxy-efavirenz is a metabolite of Efavirenz (HY-10572), a non-nucleoside HIV-1 reverse transcriptase inhibitor.
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